Subclinical versus advanced forms of alcohol-related liver disease: Need for early detection

被引:13
作者
Gomez-Medina, Concepcion [1 ]
Melo, Luma [2 ]
Marti-Aguado, David [1 ]
Bataller, Ramon [2 ,3 ]
机构
[1] Clin Univ Hosp Valencia, Med Dept, Div Gastroenterol & Hepatol, Valencia, Spain
[2] Univ Pittsburgh, Ctr Liver Dis, Div Gastroenterol, Med Ctr, Pittsburgh, PA USA
[3] Univ Pittsburgh, Div Gastroenterol Hepatol & Nutr, Med Ctr, 200 Lothrop St,BSTW Suite 1116, Pittsburgh, PA 15213 USA
关键词
Liver diseases; Alcoholic; Hepatitis; HEPATITIS-C VIRUS; GENETIC PREDISPOSITION; END-POINTS; FIBROSIS; TRANSPLANTATION; STEATOHEPATITIS; MANAGEMENT; BIOMARKERS; CIRRHOSIS; PROGNOSIS;
D O I
10.3350/cmh.2022.0017
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Alcohol-related liver disease (ALD) consists of a wide spectrum of clinical manifestations and pathological features, ranging from asymptomatic patients to decompensated cirrhosis and hepatocellular carcinoma. Patients with heavy alcohol intake and advanced fibrosis often develop a subacute form of liver failure called alcohol-induced hepatitis (AH). Globally, most patients with ALD are identified at late stages of the disease, limiting therapeutic interventions. Thus, there is a need for early detection of ALD patients, which is lacking in most countries. The identification of alcohol misuse is hampered by the existence of alcohol underreporting by many patients. There are useful biomarkers that can detect recent alcohol use. Moreover, there are several non-invasive techniques to assess the presence of advanced fibrosis among patients with alcohol misuse, which could identify patients at high risk of liver related events or early death. In this review, we discuss differences between early stages of ALD and AH as the cornerstone of advanced forms. A global overview of epidemiological, anthropometric, clinical, analytical, histological, and molecular differences is summarized in this article. We propose that campaigns aimed at identifying patients with subclinical forms can prevent the development of life-threatening forms. (Clin Mol Hepatol 2023;29:1-15)
引用
收藏
页码:1 / 15
页数:16
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